Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Natalya A Solovyevа"'
Autor:
Nikolay A Barashkov, Vera G Pshennikova, Olga L Posukh, Fedor M Teryutin, Aisen V Solovyev, Leonid A Klarov, Georgii P Romanov, Nyurgun N Gotovtsev, Andrey A Kozhevnikov, Elena V Kirillina, Oksana G Sidorova, Lena M Vasilyevа, Elvira E Fedotova, Igor V Morozov, Alexander A Bondar, Natalya A Solovyevа, Sardana K Kononova, Adyum M Rafailov, Nikolay N Sazonov, Anatoliy N Alekseev, Mikhail I Tomsky, Lilya U Dzhemileva, Elza K Khusnutdinova, Sardana A Fedorova
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0156300 (2016)
Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause of hearing impairment (HI). More than 300 allelic variants have been identified in the GJB2 gene. Spectrum and allelic frequencies of the GJB2 gene vary signifi
Externí odkaz:
https://doaj.org/article/f81ef01b7f9f4787a28282561df238bc
Autor:
Elvira E. Fedotova, Oksana G. Sidorova, Aisen V. Solovyev, Sardana A. Fedorova, Lena M. Vasilyevа, Natalya A. Solovyevа, Anatoliy N. Alekseev, Olga L. Posukh, Nyurgun N. Gotovtsev, Andrey A. Kozhevnikov, Sardana K. Kononova, Georgii P. Romanov, Fedor M. Teryutin, Igor Morozov, Alexander A. Bondar, N. N. Sazonov, Mikhail I. Tomsky, Elena V. Kirillina, Elza Khusnutdinova, A.M. Rafailov, Lilya U. Dzhemileva, Nikolay A. Barashkov, V.G. Pshennikova, Leonid A. Klarov
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 5, p e0156300 (2016)
PLoS ONE, Vol 11, Iss 5, p e0156300 (2016)
Pathogenic variants in the GJB2 gene, encoding connexin 26, are known to be a major cause of hearing impairment (HI). More than 300 allelic variants have been identified in the GJB2 gene. Spectrum and allelic frequencies of the GJB2 gene vary signifi